# LACTULOSE

NDC: 17856-0874
Generic name: Lactulose
Labeler / Manufacturer: Atlantic Biologicals Corp.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20191203

FDA application: ANDA074623

## Active ingredients

- LACTULOSE: 10 g/15mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17856-0874"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0874
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3fb6e908-893c-5a57-e063-6294a90a1bfc